<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu Y</submitter><funding>Public Welfare Foundation of Ningbo City</funding><funding>Li Dak Sum Yip Yio Chin Kenneth Li  Marine Biopharmaceutical Development Fund</funding><funding>National Natural Science Foundation of China</funding><funding>Zhejiang Basic Public Welfare Research Project</funding><funding>Higher Education Discipline Innovation Project</funding><funding>Ningbo Key Science and Technology Development Program</funding><pagination>9909-9916</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8945076</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(11)</volume><pubmed_abstract>Two rare tetracyclic skeleton alkaloids named perinadines B and C (&lt;b>1&lt;/b> and &lt;b>2&lt;/b>) were isolated as mixtures of epimers from the marine-derived &lt;i>Aspergillus&lt;/i> sp. LS116 driven by molecular networking. The planar structures of &lt;b>1&lt;/b> and &lt;b>2&lt;/b> were characterized by comprehensive spectroscopic data. Additionally, compounds &lt;b>1&lt;/b> and &lt;b>2&lt;/b> showed moderate &lt;i>in vitro&lt;/i> antibacterial activity against &lt;i>Bacillus subtilis&lt;/i> with minimum inhibitory concentration values of 32 and 64 μg/mL, respectively. Besides, both of the compounds were evaluated for anti-inflammatory activities in an &lt;i>in vivo&lt;/i> zebra fish model.</pubmed_abstract><journal>ACS omega</journal><pubmed_title>Molecular Networking-Driven Discovery of Antibacterial Perinadines, New Tetracyclic Alkaloids from the Marine Sponge-Derived Fungus &lt;i>Aspergillus&lt;/i> sp.</pubmed_title><pmcid>PMC8945076</pmcid><funding_grant_id>2021Z046</funding_grant_id><funding_grant_id>42176101</funding_grant_id><funding_grant_id>41706167</funding_grant_id><funding_grant_id>42006104</funding_grant_id><funding_grant_id>LGF22B020002</funding_grant_id><funding_grant_id>D16013</funding_grant_id><funding_grant_id>2021S059</funding_grant_id><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>He S</pubmed_authors><pubmed_authors>Wu B</pubmed_authors><pubmed_authors>Yan X</pubmed_authors><pubmed_authors>Ding L</pubmed_authors><pubmed_authors>Shi Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Molecular Networking-Driven Discovery of Antibacterial Perinadines, New Tetracyclic Alkaloids from the Marine Sponge-Derived Fungus &lt;i>Aspergillus&lt;/i> sp.</name><description>Two rare tetracyclic skeleton alkaloids named perinadines B and C (&lt;b>1&lt;/b> and &lt;b>2&lt;/b>) were isolated as mixtures of epimers from the marine-derived &lt;i>Aspergillus&lt;/i> sp. LS116 driven by molecular networking. The planar structures of &lt;b>1&lt;/b> and &lt;b>2&lt;/b> were characterized by comprehensive spectroscopic data. Additionally, compounds &lt;b>1&lt;/b> and &lt;b>2&lt;/b> showed moderate &lt;i>in vitro&lt;/i> antibacterial activity against &lt;i>Bacillus subtilis&lt;/i> with minimum inhibitory concentration values of 32 and 64 μg/mL, respectively. Besides, both of the compounds were evaluated for anti-inflammatory activities in an &lt;i>in vivo&lt;/i> zebra fish model.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2026-05-30T15:02:52.581Z</modification><creation>2025-04-04T23:04:39.529Z</creation></dates><accession>S-EPMC8945076</accession><cross_references><pubmed>35350304</pubmed><doi>10.1021/acsomega.2c00402</doi></cross_references></HashMap>